R R Nuritdinova, E. B. Zh., O. R. Ya., K A Zakhidov, Tadjimukhamedov Kh.S.
{"title":"麦基那唑啉酮氨基酶衍生物的化学选择性合成及其x射线研究","authors":"R R Nuritdinova, E. B. Zh., O. R. Ya., K A Zakhidov, Tadjimukhamedov Kh.S.","doi":"10.29055/JCCS/703","DOIUrl":null,"url":null,"abstract":"The method for chemoselective synthesis of aminobenzylic derivative of the alkaloid mackinazolinone was developed and studied its structurein the crystal. It was found that reduction of Schiff base (intermediate, 4) by sodium borohydride at room temperature goes selectively through reduction only of azomethine (N=CH) bond; wherein does not affect the C=N double bond.","PeriodicalId":15337,"journal":{"name":"Journal of Chemistry and Chemical Sciences","volume":"83 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2019-03-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":"{\"title\":\"Chemoselective Synthesis of Aminobenzylic Derivative of Mackinazolinone and its X-ray Investigations\",\"authors\":\"R R Nuritdinova, E. B. Zh., O. R. Ya., K A Zakhidov, Tadjimukhamedov Kh.S.\",\"doi\":\"10.29055/JCCS/703\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"The method for chemoselective synthesis of aminobenzylic derivative of the alkaloid mackinazolinone was developed and studied its structurein the crystal. It was found that reduction of Schiff base (intermediate, 4) by sodium borohydride at room temperature goes selectively through reduction only of azomethine (N=CH) bond; wherein does not affect the C=N double bond.\",\"PeriodicalId\":15337,\"journal\":{\"name\":\"Journal of Chemistry and Chemical Sciences\",\"volume\":\"83 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2019-03-04\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Chemistry and Chemical Sciences\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.29055/JCCS/703\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Chemistry and Chemical Sciences","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.29055/JCCS/703","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Chemoselective Synthesis of Aminobenzylic Derivative of Mackinazolinone and its X-ray Investigations
The method for chemoselective synthesis of aminobenzylic derivative of the alkaloid mackinazolinone was developed and studied its structurein the crystal. It was found that reduction of Schiff base (intermediate, 4) by sodium borohydride at room temperature goes selectively through reduction only of azomethine (N=CH) bond; wherein does not affect the C=N double bond.